Canonical Allele Identifier: CA2335054642
Gene: RYR1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.38502798_38502810delinsCAGGGGCAGGGGG , CM000681.2:g.38502798_38502810delinsCAGGGGCAGGGGG GRCh38
NC_000019.9:g.38993438_38993450delinsCAGGGGCAGGGGG , CM000681.1:g.38993438_38993450delinsCAGGGGCAGGGGG GRCh37
NC_000019.8:g.43685278_43685290delinsCAGGGGCAGGGGG NCBI36
NG_008866.1:g.74099_74111delinsCAGGGGCAGGGGG , LRG_766:g.74099_74111delinsCAGGGGCAGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000599547.6:c.7835+71_7836-70delinsCAGGGGCAGGGGG ENSP00000471601.2:n.7835+71_7836-70delinsCAGGGGCAGGGGG
ENST00000359596.8:c.7835+71_7836-70delinsCAGGGGCAGGGGG MANE Select ENSP00000352608.2:n.7835+71_7836-70delinsCAGGGGCAGGGGG
ENST00000355481.8:c.7835+71_7836-70delinsCAGGGGCAGGGGG ENSP00000347667.3:n.7835+71_7836-70delinsCAGGGGCAGGGGG
ENST00000359596.7:c.7835+71_7836-70delinsCAGGGGCAGGGGG ENSP00000352608.2:n.7835+71_7836-70delinsCAGGGGCAGGGGG
ENST00000360985.7:c.7832+71_7833-70delinsCAGGGGCAGGGGG ENSP00000354254.4:n.7832+71_7833-70delinsCAGGGGCAGGGGG
ENST00000594335.5:c.1287+71_1288-70delinsCAGGGGCAGGGGG
NM_000540.2:c.7835+71_7836-70delinsCAGGGGCAGGGGG , LRG_766t1:c.7835+71_7836-70delinsCAGGGGCAGGGGG NP_000531.2:n.7835+71_7836-70delinsCAGGGGCAGGGGG
NM_001042723.1:c.7835+71_7836-70delinsCAGGGGCAGGGGG NP_001036188.1:n.7835+71_7836-70delinsCAGGGGCAGGGGG
XM_006723317.1:c.7835+71_7836-70delinsCAGGGGCAGGGGG XP_006723380.1:n.7835+71_7836-70delinsCAGGGGCAGGGGG
XM_006723319.1:c.7835+71_7836-70delinsCAGGGGCAGGGGG XP_006723382.1:n.7835+71_7836-70delinsCAGGGGCAGGGGG
XM_011527204.1:c.7832+71_7833-70delinsCAGGGGCAGGGGG XP_011525506.1:n.7832+71_7833-70delinsCAGGGGCAGGGGG
XM_011527205.1:c.7835+71_7836-70delinsCAGGGGCAGGGGG XP_011525507.1:n.7835+71_7836-70delinsCAGGGGCAGGGGG
XM_006723317.2:c.7835+71_7836-70delinsCAGGGGCAGGGGG XP_006723380.1:n.7835+71_7836-70delinsCAGGGGCAGGGGG
XM_006723319.2:c.7835+71_7836-70delinsCAGGGGCAGGGGG XP_006723382.1:n.7835+71_7836-70delinsCAGGGGCAGGGGG
XM_011527205.2:c.7835+71_7836-70delinsCAGGGGCAGGGGG XP_011525507.1:n.7835+71_7836-70delinsCAGGGGCAGGGGG
XR_001753735.1:n.7918+71_7919-70delinsCAGGGGCAGGGGG
NM_000540.3:c.7835+71_7836-70delinsCAGGGGCAGGGGG MANE Select NP_000531.2:n.7835+71_7836-70delinsCAGGGGCAGGGGG
NM_001042723.2:c.7835+71_7836-70delinsCAGGGGCAGGGGG NP_001036188.1:n.7835+71_7836-70delinsCAGGGGCAGGGGG